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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345266Generated: October 30, 2026

Water → 1-Cyclopentene-1-acetic acid, 2,3,3-trimethyl-

https://huagongshe.com/reaction/345266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantSodium DichromateHCID 25408—
Reactant(2,3,3-Trimethylcyclopent-1-en-1-yl)acetaldehydeHCID 19810361—
SolventAcetoneHCID 180—
Product1-Cyclopentene-1-acetic acid, 2,3,3-trimethyl-HCID 12302351—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution was made of β-campholenic aldehyde (150 g) in acetone (2 liters) and cooled to 0° C. Oxidizing agent was prepared from 169 ml conc. sulfuric acid, 736 ml water and 292 g of sodium dichromate (Na2Cr2O7.2H2O). The reagent (375 ml) was added to the solution at 0° C. over a period of 30 minutes. After an additional 15 minutes at 0° C. the acetone was removed by decantation and the residual chromium salts were washed with an additional 200 ml acetone. The combined acetone solution was concentrated, the residue taken up in 10% aqueous sodium hydroxide (1 liter) and the solution washed with CH2Cl2 (2×1 liter). The aqueous phase was acidified with 25% sulfuric acid followed by extraction with CH2Cl2 (2×1 liter). Concentration of the dried CH2Cl2 solution yielded an oil (73 g) which was distilled under reduced pressure to give 53 g of a yellowish liquid; bp 102° C. @ 1.1 mm Hg; crystallized upon standing; analysis: (CW 20M fused silica column, 190° C.) 96% β-campholenic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057158
Source datasetuspto-grants-1991_10
ORD IDord-9cad72a81af54bd3bc14c40b376eade5
Source noteuspto-grants-1991_10